过电位
析氧
电解
分解水
可再生能源
电解水
催化作用
阳极
化学
材料科学
化学工程
纳米技术
工艺工程
生化工程
电极
电化学
光催化
物理化学
工程类
电气工程
电解质
生物化学
作者
Feng Zeng,Chalachew Mebrahtu,Longfei Liao,Anna Katharina Beine,Regina Palkovits
标识
DOI:10.1016/j.jechem.2022.01.025
摘要
Recently, H2 has attracted increasing attention as green energy carrier holding the possibility to replace fossil fuel-based energy sources and thereby reduce CO2 emissions. Green hydrogen can be generated by water electrolysis using renewable energies like wind and solar power. When it is combusted, only water forms as by-product. However, the efficiency of water electrolysis is hampered by the anodic oxygen evolution reaction (OER) because of the slow kinetics which leads to a high overpotential. Therefore, many catalysts have been developed for OER to facilitate the kinetics and reduce the overpotential. In addition to electrocatalytic activity, the stability of the catalysts is imperative for industrial application and has been intensively studied. In this review, we cover recent findings on the stability and deactivation mechanisms of OER catalysts. We discuss the correlation between OER activity and stability, methodologies and experimental techniques to study the stability and deactivation as well as the deactivation mechanisms, together with factors influencing stability. Furthermore, strategies for stabilizing and regenerating OER catalysts as well as methods to predict stability are summarized. Finally, the review highlights emerging methodologies yet to be explored and future directions of stability studies and the design of highly stable OER catalysts.
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